A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18251186



Internal ID20818226
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:49737586..49958244hg38UCSC Ensembl
chr1:50203258..50423916hg19UCSC Ensembl
Cytoband1p33
Allele length
AssemblyAllele length
hg38220659
hg19220659
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6539866
Supporting Variants
Samples
Known GenesAGBL4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18251186
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer